Enzymatic debranching is a key determinant of the xylan-degrading activity of family AA9 lytic polysaccharide monooxygenases

Background Previous studies have revealed that some Auxiliary Activity family 9 (AA9) lytic polysaccharide monooxygenases (LPMOs) oxidize and degrade certain types of xylans when incubated with mixtures of xylan and cellulose. Here, we demonstrate that the xylanolytic activities of two xylan-active LPMOs, TtLPMO9E and TtLPMO9G from Thermothielavioides terrestris, strongly depend on the presence of xylan substitutions. Results Using mixtures of phosphoric acid-swollen cellulose (PASC) and wheat arabinoxylan (WAX), we show that removal of arabinosyl substitutions with a GH62 arabinofuranosidase resulted in better adsorption of xylan to cellulose, and enabled LPMO-catalyzed cleavage of this xylan. Furthermore, experiments with mixtures of PASC and arabinoglucuronoxylan from spruce showed that debranching of xylan with the GH62 arabinofuranosidase and a GH115 glucuronidase promoted LPMO activity. Analyses of mixtures with PASC and (non-arabinosylated) beechwood glucuronoxylan showed that GH115 action promoted LPMO activity also on this xylan. Remarkably, when WAX was incubated with Avicel instead of PASC in the presence of the GH62, both xylan and cellulose degradation by the LPMO9 were impaired, showing that the formation of cellulose–xylan complexes and their susceptibility to LPMO action also depend on the properties of the cellulose. These debranching effects not only relate to modulation of the cellulose–xylan interaction, which influences the conformation and rigidity of the xylan, but likely also affect the LPMO–xylan interaction, because debranching changes the architecture of the xylan surface. Conclusions Our results shed new light on xylanolytic LPMO9 activity and on the functional interplay and possible synergies between the members of complex lignocellulolytic enzyme cocktails. These findings will be relevant for the development of future lignocellulolytic cocktails and biomaterials. Supplementary Information The online version contains supplementary material available at 10.1186/s13068-022-02255-2.


Background
Polysaccharide-degrading lytic polysaccharide monooxygenases (LPMOs) are metalloenzymes whose activity depends on reduction of a single Cu atom in the catalytic center and an oxygen co-substrate (H 2 O 2 , O 2 ) [1][2][3][4]. LPMOs belonging to Auxiliary Activity family 9 (AA9, [5]), LPMO9s, oxidize their cellulosic or hemicellulosic substrates either at C1, resulting in the formation of lactones that are in equilibrium with aldonic acids, or at C4, resulting in the formation of 4-ketoaldoses that are in equilibrium with gemdiols. Some LPMO9s produce mixtures of C1-and C4-oxidized products and may thus generate double oxidized products, whereas in some cases, oxidation at C6 has also been observed [6][7][8][9][10]. LPMOs were discovered in 2010 [1] and have since gathered wide interest in the industrial biotechnology field, due to their ability to significantly boost the activity of cellulases in the cellulolytic enzyme cocktails that are used to convert carbohydrates in renewable biomass to fermentable sugars for production of fuels and chemicals [11,12]. The role of LPMO9s in saccharification of cellulose has been studied in much detail, as reviewed in e.g. [4] and [12]. It is becoming increasingly clear that certain LPMO9s, next to acting on linear and crystalline cellulose, can also act on one or more hemicelluloses, such as xyloglucan, glucomannan and arabinoxylan, either alone or when adsorbed to cellulose [8,[13][14][15][16][17]. Notably, these hemicelluloses are heteropolymers, often with substitution groups on the main chain, which raises interesting questions regarding the substrate specificity of LPMO9s and their interplay with other enzymes involved in hemicellulose debranching and depolymerization. Secondary plant cell walls, the major constituents of plant biomass, are primarily comprised of cellulose, various hemicelluloses, and lignin. Their chemical nature and supramolecular structure make plant cell walls strong biocomposites that are resistant to chemical, biotic, and physical stresses. The recalcitrance of cellulose comes from its (largely) crystalline structure that is stabilized by numerous hydrogen bonds, hydrophobic interactions, and Van der Waals forces. Hemicelluloses share with cellulose a backbone of β-(1,4)-linked monosaccharides but lack a crystalline lattice and are heteropolymeric with numerous different monosaccharide building blocks. In addition, hemicelluloses show large variation in molecular composition and structure between plants and even tissues [18,19]. Hemicelluloses referred to as xylans are comprised of a backbone of β-1,4-linked xylopyranosyl monomers that are often substituted by decorating sugars such as arabinose and/or (methyl)glucuronic acid ((Me) GlcA) and may carry acetyl groups [18][19][20]. In accordance with their predominating substitutions, xylans are often referred to as glucuronoxylan (GX), arabinoxylan (AX) or arabinoglucuronoxylan (AGX).
Although further corroboration is needed, it is known that xylans have a tethering function in plant cell walls by adsorbing to cellulose, and that adsorption strength depends on both the degree and pattern of substitution. The occurrence of regular motifs of glycosyl substitutions and acetylations has been reported for xylans from angiosperms [21][22][23][24] and gymnosperms [25,26], and these motifs are thought to play an important role in modulating the interaction of hemicelluloses with cellulose and lignin [24,[27][28][29]. Current data indicate that adsorption is strongest for xylans that have a low degree of substitution [30][31][32] or a regular substitution pattern [23,26,27]. Xylans with no or very few substitutions tend to aggregate to each other and/or bind strongly to cellulose [31][32][33]. It has been shown that xylan adsorption to cellulose also depends on key properties of the latter, such as cellulose crystal geometry, surface area, porosity, and crystallinity [26,30,34].
Studies of LPMO9s from Neurospora crassa [13,16], Myceliophthora thermophila [14,35], Podospora anserina [15], Malbranchea cinnamomea [8] and Thermothielavioides terrestris [36] have revealed activity of these enzymes on hemicelluloses, such as xyloglucan from tamarind seeds, glucomannan from konjac, glucuronoxylan from beech and birchwood, and oat spelt arabinoxylan. In the case of xylans, LPMO9 activity, i.e., reductant-dependent generation of oxidized products, has only been convincingly demonstrated when using reaction mixtures that also contain cellulose. This dependency on the presence of cellulose has been explained [8,14,16,36] by an expected conformational change of the xylan, which in solution adopts a threefold helical conformation but in combination with cellulose adopts a more stretched twofold helical structure that allows strong adsorption to cellulose [25][26][27][28]37]. The resulting flatter surface of the xylan-cellulose co-polymeric structure seems well-adapted to the flat substrate-binding surfaces of xylan-active LPMO9s and likely mimics the ultrastructure of these polysaccharides in native plant cell walls.
T. terrestris is an extremophilic ascomycetous filamentous fungus that encodes and utilizes a plethora of lignocellulose active enzymes, including numerous AA9 LPMOs [38,39]. In a previous study, we have characterized six LPMO9s from T. terrestris LPH172, three of which showed activity toward beechwood, birchwood and/or spruce xylans, only when these xylans were combined with phosphoric acid-swollen cellulose (PASC) [36]. Interestingly, our study revealed major substitutiondependent differences between the xylan-active LPMOs. For example, TtLPMO9E showed activity on both acetylated and non-acetylated glucuronoxylan, but not on arabinoglucuronoxylan, whereas TtLPMO9G showed (weaker) activity on non-acetylated glucuronoxylan and on arabinoglucuronoxylan [36]. None of these xylanactive LPMOs showed activity on wheat arabinoxylan (WAX), in line with early observations by Frommhagen et al. [14] who concluded that xylan-active MtLPMO9A did not act on this highly substituted xylan type (WAX that had a 62:38 xylose:arabinose ratio). Taken together, the considerations and observations described above lead us to the hypothesis that the activity of LPMO9s on xylan may be modulated by debranching enzymes, such as (methyl)-glucuronidases and arabinofuranosidases, because debranching will both modulate the crucial formation of LPMO-susceptible xylan-cellulose complexes and affect the ability of the LPMO to interact with the xylan. Therefore, we set out to investigate whether LPMO9 activity on a variety of xylans (WAX, spruce arabinoglucuronoxylan (SpAGX), beechwood glucuronoxylan (BeGX)) is affected by the action of a GH62 α-arabinofuranosidase and/or a GH115 (methyl)-glucuronidase. The results show that, generally, debranching leads to increased xylanolytic activity of LPMO9s and in some cases enables LPMO9 activity on substrates for which previously no activity had been detected. We also show that the xylanolytic activity of LPMO9s depends on the type of cellulose present in the reaction mixture. Next to underpinning the (known) impact of debranching enzymes on cellulose-xylan interactions, our results support the notion that AA9 LPMOs may play a significant role in xylan degradation that may depend on the interplay with debranching enzymes. Such interplay, as well as the newly discovered activities of LPMO9s on xylans as such, will likely be relevant in the development of future lignocellulolytic enzyme cocktails for biomass processing.

The activity of TtLPMO9E on WAX is inhibited by arabinosyl substitutions
We have previously shown that TtLPMO9E is active on various xylan substrates but not on standard WAX, which is a highly substituted arabinoxylan with 38% of its monosaccharides being arabinose [36]. Next to this substrate, here referred to as WAX38 (38:62 Ara:Xyl; A/X ratio 0.61), we also tested WAX30 (30:70 Ara:Xyl; A/X ratio 0.43) and WAX22 (22:78 Ara:Xyl; A/X ratio 0.28), to assess whether reduced substitution could increase LPMO activity. Figure 1 shows the chemical structure of WAX and of the other xylan substrates (see below) used in this study.
All three WAX substrates (0.2%, w/v) were incubated with 0.2% (w/v) PASC and TtLPMO9E, using gallic acid (GA) as a reductant to drive LPMO activity. A reaction with only PASC was also conducted to generate a standard for cellulose-derived products. The results showed the expected absence of xylan-derived products for the reactions with WAX30 and WAX38 (Fig. 2). On the other hand, the reaction with PASC and WAX22 generated multiple (arabino)xylan-derived products. These peaks were most evident in the 12-25 min region (Fig. 2). Of note, these products were not observed in control reactions without LPMO or reductant (Additional file 1: Fig.  S1), which shows that they are indeed the products of LPMO activity. Taken together, the results clearly show that arabinose substitutions inhibit the activity of TtLP-MO9E on WAX, but that TtLPMO9E has activity on WAX with lower degrees of substitution.
Next to the effect of substitutions on the WAX-cellulose interaction, variation in the length of the xylan chains could also play a role, with longer chains showing improved adsorption [30], which could increase susceptibility to LPMO action. Based on the data provided by the manufacturer, WAX30 has longer chains than WAX38, while the former was not a better substrate for the LPMO. Therefore, we conclude that debranching, and not chain length, explains why WAX22 is the best substrate for the LPMO, although the effect of molecular weight cannot be completely excluded based on our data.
Due to the complexity of the HPAEC-PAD chromatograms and the lack of suitable analytical standards for arabinoxylan-oligomers, the identity of the LPMOgenerated WAX22-derived reaction products could not be determined for the chromatograms. MALDI-TOF MS analysis was not done for these initial experiments with various WAX types. Below, we describe MALDI-TOF MS analyses of other samples of LPMO-treated WAX, which show that mixtures of LPMO-generated WAX-derived reaction products contain multiple species with masses corresponding to native and oxidized xylo-oligomers.

The activity of TtLPMO9E on WAX22 and WAX38 increases upon debranching with UmGH62 α-l-arabinofuranosidase
To further test the hypothesis that TtLPMO9E activity on WAX is affected by arabinose substitutions and to investigate whether it was possible to further increase TtLPMO9E activity on WAX, we tested the impact of adding a GH62 arabinofuranosidase to LPMO reactions with PASC and WAX38 or PASC and WAX22. The enzyme used, UmGH62, removes α-l-arabinofuranose from singly substituted xylose residues [42] and has a preference for α-1,2 substitutions relative to α-1,3 substitutions according to the enzyme supplier [43]. Figure 3 shows that addition of UmGH62 to the reaction mixture enabled TtLPMO9E to degrade WAX38 (Fig. 3a) and increased the activity of the LPMO on WAX22 further (Fig. 3b). The importance of debranching for the TtLP-MO9E activity on WAX is evident from the appearance of novel product peaks, as well as peaks with higher intensities in the chromatograms for reactions with UmGH62 compared to reactions without UmGH62. MALDI-TOF MS analysis of products generated from WAX38 in the absence or presence of the GH62 confirmed the importance of the GH62 for LPMO-catalyzed WAX38 degradation and showed that the product mixture generated in the reaction with both the LPMO and the GH62 contains multiple species with masses corresponding to native and oxidized xylo-oligomers (Additional file 1: Fig. S2). The chromatograms of Fig. 3 show similar, albeit not identical, product patterns for reactions with WAX38 and WAX22; differences appear in the 5-10 min region of the chromatograms (Fig. 3a, b), where the shortest and least substituted products elute. A simple dose-response analysis showed that the amount of UmGH62 was not limiting under the conditions used, as a tenfold reduction of the amount of UmGH62 in the experiment with PASC + WAX22 only had a limited effect on product formation (Fig. 3c). Control reactions where the LPMO or the reductant were replaced by water did not generate any LPMO-derived products (Fig. 3). Additional control reactions with only WAX38 or WAX22 (Additional file 1: Fig. S3) confirmed that the presence of a cellulosic matrix is essential for the LPMO's ability to cleave the xylan substrate.

Debranching with UmGH62 arabinofuranosidase and BoGH115A α-(methyl-) glucuronidase improves LPMO activity on spruce and beechwood glucuronoxylans
As the impact of debranching on the activity of TtLP-MO9E on WAX was evident, we analyzed if this effect also applied to other types of xylans (Fig. 1), and with   [40]). BoGH115A is expected to remove both GlcA and MeGlcA groups (here collectively referred to as (Me)GlcA) with a preference for groups attached to internal xylose residues [41], making it a good candidate for debranching SpAGX. Figure 4a shows that the addition of BoGH115A had minimal effects, if any, on the hardly detectable activity of TtLPMO9G on SpAGX. Minor, barely visible peaks in the 9-14 min elution region suggest that there may be a slight increase in activity due to the addition of BoGH115A. Addition of UmGH62 did lead to increased generation of LPMO products, eluting later (16-25 min; Fig. 4a) than the most prominent LPMO products generated from WAX (Figs. 2 and 3). This delayed elution is likely due to the presence of glucuronic acid moieties that add charge to the products, resulting in delayed elution. Most interestingly, the addition of both debranching enzymes led to a clear increase in product generation by TtLP-MOG, demonstrating a synergy between the debranching activities of BoGH115A and UmGH62 and a need to remove both arabinose and MeGlcA for SpAGX to increase susceptibility to the LPMO. Of note, the potentially glucuronated LPMO products visible in the reaction with UmGH62 only were no longer detected in the reaction that also contained BoGH115A. Control reactions without the reductant or without the LPMO (Additional file 1: Fig. S4) confirmed that the products visible in Fig. 4a were indeed a result of LPMO action. Control reactions containing BoGH115A (Additional file 1: Fig.  S4) showed a major peak eluting at 7 min, which likely is the released MeGlcA.
In our previous study in which we identified xylanactive LPMO9s from T. terrestris [36], TtLPMO9E showed the highest activity on several xylans, but it did not show any activity on SpAGX. Intriguingly, when both BoGH115A and UmGH62 were added to a reaction with PASC, SpAGX and TtLPMO9E, SpAGX was readily degraded (Fig. 4b), generating levels of xylan-derived  Fig. S1). Native cello-oligomers, which are present in small amounts, were not identified; they elute in the 2-11 min area and small non-annotated peaks likely belonging to such native products are visible in the 5-11 min sections of the chromatograms products that were higher than those obtained with TtLPMO9G. The product profiles obtained in the reactions containing UmGH62 and BoGH115A differed between TtLPMO9G and TtLPMO9E (Fig. 4a, b), indicating that these two LPMO9s differ in how they tolerate substitutions of the xylan backbone. The lack of dominating cellulose-derived peaks in the chromatogram for the reaction with TtLPMO9E, UmGH62 and BoGH115A (Fig. 4b) is noteworthy; this could indicate that debranched SpAGX is as good a substrate for TtLP-MO9E as PASC, or even better.
To gain further insight into product formation, soluble compounds generated by TtLPMO9G in the reaction with PASC and SpAGX in the presence of UmGH62 and BoGH115A were analyzed by MALDI-TOF MS. The results are displayed in Fig. 5a (700-1400 m/z) and Fig. 5b (1400-2100 m/z). Supporting the results from HPAEC-PAD analysis, the MS spectra showed oxidized reaction products resulting from both cellulose and xylan cleavage. The longest detectable oxidized cellooligomers contained eight glucose units, as is commonly observed due to the limited solubility of longer cellulose fragments. Products originating from xylan degradation were longer, ranging up to at least fifteen pentose monomers. Since the dehydrated masses of both xylopyranose and arabinofuranose units are 132 Da, it is not possible to distinguish if the products are linear (e.g., only xylose) or also include arabinose substitutions. The dominating xylan-derived products are monosodium adducts of native oligomers, oxidized oligomers and hydrated forms of the latter, as well as sodium salts of the hydrated forms (Fig. 5a). These product forms are commonly observed in reactions with C1-oxidizing LPMOs [44,45]. The MS analysis confirmed that the reductant-free control reaction did not yield oxidized products. In control reactions without UmGH62 and BoGH115A, only cellulose-derived products were identified (Fig. 5a, red spectrum). Of note, the mass spectra show several xylan-derived products with masses that corresponded to MeGlcA-substituted (+ 190 Da) xylooligomers. Although MALDI-TOF MS should be considered strictly qualitative, it is interesting to note that the intensities of these product peaks were much weaker than for those belonging to non-MeGlcAsubstituted products, which is to be expected considering the presence of BoGH115A in the reaction.
Previously, both TtLPMO9E and, to a much lesser extent, TtLPMO9G have been shown to be active on beechwood glucuronoxylan (BeGX) [36], which is not arabinosylated. Figure 4c shows that addition of BoGH115A to reactions with PASC and BeGX increased the activity of both TtLPMO9s. Interestingly, as also observed above, in the product profile for the reaction with TtLPMO9E and BoGH115A, cellulosic peaks were no longer dominating, again illuminating the high xylanolytic activity of this LPMO. Chromatograms for control reactions without the LPMO or the reductant (Additional file 1: Fig. S5) confirmed that product formation was catalyzed by the LPMO and demonstrated BoGH115A-catalyzed release of (Me)GlcA.

The type of cellulose affects xylanolytic LPMO9 activity
Hemicellulose adsorption onto cellulose depends also on the source and related characteristics of the cellulosic material [30,34]. For instance, Kabel et al. demonstrated in 2007 that xyloglucan adsorbed better to bacterial cellulose compared to Avicel, and hypothesized that this is due to the higher surface area of bacterial cellulose [30]. It has been shown that in PASC, solvent accessible fibril surfaces are more prominent than in Avicel [46]. To get an impression of the impact of different cellulosic substrates, we tested both Avicel and PASC as cellulose matrices in reactions with TtLPMO9E and WAX30, in the absence or presence of UmGH62. Reactions with PASC showed clear xylanolytic activity on UmGH62treated WAX30 (Fig. 6), as was to be expected based on the results of similar reactions with WAX22 and WAX38 discussed above (Fig. 3). Unexpectedly, in the reactions with Avicel, the LPMO-catalyzed degradation of WAX30 was almost completely absent (Fig. 6). Addition of PASC to the TtLPMO9E reaction with Avicel, WAX30 and UmGH62 restored LPMO activity on xylan, indicating that WAX30 was not irreversibly adsorbed onto Avicel and that WAX30 more readily adsorbs onto PASC compared to Avicel. It is worth noting that Fig. 6 also shows how addition of WAX30 to Avicel hinders LPMO9 activity on Avicel (see lower two chromatograms); this adds to the notion that WAX30 indeed binds to, and coats the Avicel fiber. Control reactions without reductant did not result in any product formation (Additional file 1: Fig.  S6).

Discussion
In the present study, the effect of xylan debranching enzymes on the xylan-degrading activity of family AA9 LPMOs was assessed for the first time. We showed that debranching of xylans can both reveal previously undiscovered xylanolytic activities of LPMOs and significantly boost previously reported activities. Similar improvements in hemicellulose degradation by debranching enzymes have previously been shown for mannanases [47] and xylanases [48][49][50], but to the best of our knowledge, such studies have not been conducted for LPMO9s prior to the present study.
Although there are studies suggesting that LPMOs may act on free xylans [51][52][53], convincing activity, i.e., reductant-dependent and with considerable oxidized product formation, has only been detected in reactions that also contain cellulose [8,14,16,36]. This shows that LPMO activity on xylan is dependent on, or at least drastically promoted by, adsorption to cellulose. Improved adsorption is expected since complete debranching of stretches of xylan and/or partial debranching resulting in an even substitution pattern both are known to promote binding of xylan onto cellulose [23,27,[30][31][32]. On the other hand, the improved LPMO9 activity upon debranching may result from improved binding of LPMOs to cellulose-adsorbed xylans, as xylan substitutions may cause steric hindrance that prevent productive binding of the LPMO. It has been shown that xylan adsorption onto cellulose tends to leave the substitutions protruding from the xylan surface on the side that is not adsorbed to cellulose [23,25,37]. While such protruding groups may prevent productive LPMO binding in some cases, they may also be recognized by LPMO9 that specifically act on certain substituted cellulosexylan co-polymeric structures. Further studies addressing the conformation of LPMO-substrate complexes are needed to gain insight into these matters. For example, it has recently been shown that sulfate half ester groups on cellulose nanocrystals hamper LPMO10 activity on such sulfated substrates [54], likely due to both steric effects and charge-related repulsion.
Based on our results presented here, and a recent study by Hegnar et al. [16], it is possible to hypothesize that (crystalline) cellulose is not necessarily the preferred substrate for all LPMO9s and that some LPMOs in fact have evolved to act on xylan. For example, we show (Fig. 4) that the soluble products generated in reactions with TtLPMO9E, BoGH115A, UmGH62 and mixtures of PASC and BeGX are not dominated by cellulose-derived products, suggesting that cellulose-bound xylan is the preferred substrate (and not PASC). Furthermore, Hegnar et al. [16], quantified oxidized cellulose-and xylanderived products generated in reactions with LPMO9s and mixtures of PASC and BeGX. They showed that for the most xylan-active LPMO analyzed in the study, NcLPMO9F, the ratio of oxidized xylan-derived products relative to oxidized cellulose-derived products was 3 to 1. One of the other tested enzymes, McLPMO9H, generated approximately equal amounts of xylan-and cellulosederived products, whereas cellulose-derived products dominated for the third enzyme investigated in the study, NcLPMO9L. All in all, it is clear that xylan-degradation can be a dominating activity of some LPMO9s, which, however, varies among different enzymes and is dependent on the type of xylan and its interaction with cellulose.
Some LPMO9s are active on multiple types of hemicelluloses. Remarkably, while activity on other hemicelluloses, such as xyloglucan, may be promoted by the presence of cellulose [17], as is the case for xylan, several LPMO9s are active on pure glucomannans and xyloglucans [8,35,55]. This variation in cellulose-dependency is likely related to variation in the rigidity and conformational state of hemicelluloses in solution and may also relate to variation in the binding affinities of LPMO9s for these substrates.
It remains to be understood how the substrates used in the work described above relate to true plant cell wall materials, which are more complex co-polymeric structures. It is likely that specific LPMOs have evolved to attack specific co-polymeric substructures in the plant cell wall, such as cellulose-bound xylan, as has been described for an AA14 LPMO [56]. In this context, the differences between the type of cellulose tested (PASC vs. Avicel, Fig. 6) is noteworthy. While we cannot fully explain why the clear boosting effect of UmGH62 on WAX30 degradation by TtLPMO9E was not present when Avicel was used as the cellulose matrix instead of PASC, this result clearly shows that the formation of LPMO-susceptible xylan-cellulose complexes also depends on the cellulose. It is also worth noting that the  a and b show the m/z regions from 700 to 1400 and from 1400 to 2100, respectively. The top spectra show reactions in the presence of reductant (GA), the middle spectra reductant free controls, and the bottom spectra are control reactions without UmGH62 and BoGH115A. Native and oxidized cellulose-derived products (Glc) are labelled blue, and native and oxidized xylan-derived products (Pen) are either labelled green (non-MeGlcA-substituted), or red (MeGlcA-substituted). Light and dark colors represent native and oxidized forms, respectively. "Pen" stands for pentose and indicates xylan-derived products, where the latter may be either linear or substituted with arabinofuranose. All labels refer to single Na-adducts. Hydrated forms of oxidized products are labeled with *, whereas the sodium salts of aldonic or carboxylic acids are labeled with #. otherwise evident degradation of Avicel by TtLPMO9E was hindered by the presence of WAX30 and UmGH62, suggesting that the WAX adsorbs onto Avicel in a way that makes both the xylan and the cellulose inaccessible to cleavage. This observation underpins variation in the co-polymeric structures that may be formed by plant polysaccharides, which translates into variation in their susceptibility to plant biomass degrading enzymes. When PASC was added to the mixture together with Avicel, WAX30 and UmGH62, both the xylan-and cellulose-degrading ability of the LPMO were restored, indicating stronger adsorption of WAX30 onto PASC. The biochemical basis for these effects is an interesting starting point for increasing the fundamental understanding of the plant cell wall and thereby putting us in a better position to understand LPMO action. Of note, these findings are also relevant for industrial biomass processing. The various methods that may be used for pretreating lignocellulosic biomass prior to enzymatic digestion will affect the structure and crystallinity of cellulose in different ways, which again may affect the degree and the nature of the association between cellulose and remaining xylan. The secretomes of lignocellulose-degrading microbes contain a plethora of enzymes that concertedly degrade complex, recalcitrant and co-polymeric substrates. LPMO encoding genes and LPMOs are key components of many such transcriptomes or secretomes, respectively [39,57,58]. The present study sheds light on a possible new type of interplay and synergy between members of these secretomes, namely, hemicellulolytic LPMOs and hemicellulose-modifying (debranching) enzymes. Interestingly, a previous analysis of the transcriptomes of T. terrestris grown on three different substrates, showed that one of the two GH62 arabinofuranosidase genes is highly upregulated during growth on rice straw (but not during growth on Avicel or beechwood xylan) [39]. Findings like this substantiate the hypothesis that LPMOs might work in concert with xylan-(or other hemicellulose-) debranching enzymes in Nature.
We believe that the connections between LPMOs and hemicellulose debranching enzymes unraveled in the present study may be used to optimize industrial biorefining of lignocellulosic biomass, to produce either fermentable sugars or biomaterials. It is well-known that cellulose-bound recalcitrant xylan inhibits cellulolytic enzyme activity and increases the recalcitrance of lignocellulosic materials [59,60]. Removal of xylan by LPMOs may improve subsequent saccharification of cellulose and could also be used to produce cleaner cellulose fiberbased biomaterials. It would be interesting to study the effect of debranching enzymes on the impact of LPMOs in lignocellulolytic cocktails. Of note, when doing so, enzyme dosing must be carefully considered as excess debranching may initiate xylan aggregation and/or promote excess cellulase-inhibiting adsorption of xylan onto cellulose. An even deeper molecular-level understanding of how various plant cell wall polymers interact [61,62] would help in such endeavors.

Conclusions
A key to solving problems related to the recalcitrance of lignocellulosic biomass and establishing economically feasible biorefineries lies in the optimized use of lytic polysaccharide monooxygenases. So far, the focus has mainly been on AA9 family LPMOs and their role in degrading crystalline cellulose. In the present study, we demonstrated for the first time that xylan debranching enzymes like a GH62 arabinofuranosidase and a GH115 (methyl)glucuronidase increased and even revealed previously hidden xylan-degrading activities of two TtLPMO9s on xylan-PASC mixtures as the celluloseadsorbed conformation of debranched xylan was likely more accessible to LPMOs. Our findings indicate that in Nature, where a concert of biomass degrading enzymes are present and xylan is found in complex with cellulose, some AA9 LPMOs have likely high capacity to degrade not only cellulose but also xylan. This study illuminates high xylanolytic capabilities of AA9 LPMOs and their functional interplay and likely synergies between other components of complex lignocellulolytic cocktails. Our study paves a way for optimizing the substrate specificities of AA9 LPMOs in future lignocellulolytic cocktails and opens possibilities for exploiting xylanolytic LPMO9s in the production of future biomaterials.

Production and purification of TtLPMO9E and TtLPMO9G
Both TtLPMO9E and TtLPMO9G were heterologously produced, purified and tested for activity as described previously [36]. Shortly, the gene encoding TtLPMO9E, with its natural signal peptide and with no tags attached, was cloned into the pPINK-GAP system [63], and expressed in Pichia pastoris PichiaPink strain 4 (Invitrogen, Waltham, MA, United States). The cultivation was carried out for 4 days in 1 L YPD in a 5 L baffled shake flask at 250 rpm and 29 °C. The enzyme was purified from the culture supernatant using ion exchange chromatography as described previously [36]. The TtLPMO9G gene was cloned into the pPICZαA vector and expressed in P. pastoris SMD1168H (Invitrogen, Waltham, MA, United States). The expression strain was grown for 5 days in 750 mL BMMY medium in a 5 L baffled shake flask with supplementation of both 1% (v/v) methanol and 1% (w/v) sorbitol at timepoint zero and then every 24 h afterward (our previous work [36] showed that sorbitol supplementation increases LPMO yields with this expression system). The cultivation of this strain was carried out at 200 rpm and 30 °C. The TtLPMO9G gene included a C-terminal His 6 tag and the protein was purified using gravity flow IMAC. The purities of both enzymes were confirmed using SDS-PAGE and protein concentrations were determined from A 280 measurements using the respective theoretical extinction coefficients. The pure enzymes were filtered through 0.22 µm Fisherbrand ™ sterile PES filters (Thermo Fisher Scientific, Waltham, MA, USA) and stored at 4 °C in 50 mM BisTris-HCl buffer, pH 6.5.

UmGH62 and BoGH115A
The Ustilago maydis GH62 α-l-arabinofuranosidase with the product code E-ABFUM was purchased from Megazyme (Bray, Ireland). The high purity recombinant enzyme was supplied as a ~ 200 U/mL suspension in 3.2 M ammonium sulphate and has a pH optimum of 5.0 and temperature optimum of 40 °C. According to Megazyme, one unit of α-l-arabinfuranosidase activity is defined as the amount of enzyme required to release 1 µM of arabinose per minute from 10 mg/mL wheat arabinoxylan in 100 mM sodium acetate buffer at pH 5.0 and 40 °C [43]. The enzyme was stored at 4 °C. A recombinantly produced GH115 α-(methyl)glucuronidase from Bacteroides ovatus with product code CZ0311 was purchased from NZYTech (Lisbon, Portugal). BoGH115A was supplied at 1 mg/mL in 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl 2 and 25% (v/v) glycerol. The ≥ 90% pure BoGH115A was reported to have a pH optimum of 7.0 and a temperature optimum of 37 °C. The enzyme was stored at − 20 °C. For both enzymes, protein concentrations were analyzed using A 280 measurements and the theoretical extinction coefficients.

Enzymatic reactions
All reactions, except for those with Avicel instead of PASC, were set up in triplicates with 100 µL reaction volume in 1.5 mL Eppendorf tubes and incubated in orbital thermomixers set at 1000 rpm. Reactions with Avicel were set up with a 500 µL final volume, in duplicates, in 2 mL Eppendorf tubes, using head-to-tail mixing at 60 rpm. All reactions were carried out in 50 mM BisTris-HCl buffer at pH 6.5 and at 40 °C, which are conditions that favor LPMO activity, while being suboptimal for